DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Haaxma CA, Crow YJ, van Steensel MA. et al.
A de novo p.Asp18Asn mutation in TREX1 in a patient with Aicardi-Goutières syndrome.
Am J Med Genet A 2010;
152A (10) 2612-2617
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